Jabbour Elias, Cortes Jorge, Kantarjian Hagop
Department of Leukemia, The University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030, USA.
Oncology (Williston Park). 2007 May;21(6):653-62; discussion 663-4, 667-8.
The development of imatinib mesylate (Gleevec), a tyrosine kinase inhibitor targeted against the causative Bcr-Abl protein in chronic myeloid leukemia (CML), has resulted in hematologic and cytogenetic remissions in all phases of CML. Following imatinib treatment, more than 90% of patients obtain complete hematologic response, and 70% to 80% achieve a complete cytogenetic response. With 5 years of follow-up, the data are very encouraging, exhibiting a major change in the natural history of the disease. The understanding of at least some of the mechanisms of resistance to imatinib has led to a rapid development of new agents that may overcome this resistance. Combination strategies are currently being investigated in preliminary clinical studies and may prove to be useful. Overall, there are an increasing number of treatment options now available for patients with CML.
甲磺酸伊马替尼(格列卫)是一种靶向慢性粒细胞白血病(CML)致病的Bcr - Abl蛋白的酪氨酸激酶抑制剂,它已使CML各阶段患者实现血液学和细胞遗传学缓解。接受伊马替尼治疗后,超过90%的患者获得完全血液学缓解,70%至80%的患者实现完全细胞遗传学缓解。经过5年的随访,数据非常令人鼓舞,显示出该疾病自然史的重大变化。对伊马替尼耐药机制的至少部分理解促使了可能克服这种耐药性的新药物的快速研发。联合治疗策略目前正在初步临床研究中进行探索,可能会被证明是有用的。总体而言,现在CML患者有越来越多的治疗选择。